Poissons marins des îles subantarctiques
212 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Duhamel et al. (2005) | 129 | 13,48% | 124 | 47,69% | 121 | 47,64% | 124 | 48,44% |
| Béarez et al. (2017) | 31 | 3,24% | 30 | 11,54% | 30 | 11,81% | 28 | 10,94% |
| Fricke et al. (2011) | 20 | 2,09% | 20 | 7,69% | 20 | 7,87% | 19 | 7,42% |
| Walbaum (1792) | 12 | 1,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1848) | 11 | 1,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dettaï et al. (2011) | 10 | 1,04% | 10 | 3,85% | 10 | 3,94% | 10 | 3,91% |
| Shandikov (2011) | 10 | 1,04% | 10 | 3,85% | 10 | 3,94% | 10 | 3,91% |
| Chernova & Duhamel (2003) | 9 | 0,94% | 9 | 3,46% | 7 | 2,76% | 9 | 3,52% |
| Duhamel & King (2007) | 9 | 0,94% | 9 | 3,46% | 9 | 3,54% | 9 | 3,52% |
| Ifremer (2009) | 9 | 0,94% | 7 | 2,69% | 7 | 2,76% | 6 | 2,34% |
| Lacepède (1803) | 9 | 0,94% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fourt et al. (2017) | 8 | 0,84% | 8 | 3,08% | 8 | 3,15% | 6 | 2,34% |
| Moreau & Duhamel (1997) | 8 | 0,84% | 8 | 3,08% | 8 | 3,15% | 8 | 3,12% |
| Siu et al. (2017) | 8 | 0,84% | 7 | 2,69% | 7 | 2,76% | 7 | 2,73% |
| Moller & King (2007) | 7 | 0,73% | 7 | 2,69% | 7 | 2,76% | 7 | 2,73% |
| Blanc (1954) | 6 | 0,63% | 2 | 0,77% | 2 | 0,79% | 2 | 0,78% |
| Günther (1866) | 6 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1758) | 6 | 0,63% | 3 | 1,15% | 3 | 1,18% | 3 | 1,17% |
| Pallas [1814] | 6 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rafinesque Schmaltz (1810) | 6 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shandikov (1995) | 6 | 0,63% | 6 | 2,31% | 6 | 2,36% | 6 | 2,34% |
| Soubeyran (2008) | 6 | 0,63% | 5 | 1,92% | 5 | 1,97% | 5 | 1,95% |
| Frenot et al. (2005) | 5 | 0,52% | 4 | 1,54% | 4 | 1,57% | 4 | 1,56% |
| Fricke et al. (2009) | 5 | 0,52% | 5 | 1,92% | 5 | 1,97% | 5 | 1,95% |
| Gmelin (1789) | 5 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1878) | 5 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gilchrist (1906) | 4 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1894) | 4 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kenaley (2007) | 4 | 0,42% | 4 | 1,54% | 4 | 1,57% | 4 | 1,56% |
| Nielsen et al. (2008) | 4 | 0,42% | 4 | 1,54% | 4 | 1,57% | 4 | 1,56% |
| Nilsson (1832) | 4 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Risso (1827) | 4 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vaillant (1888) | 4 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
| Andriashev (1982) | 3 | 0,31% | 3 | 1,15% | 2 | 0,79% | 3 | 1,17% |
| Barbosa du Bocage & Brito Capello (1864) | 3 | 0,31% | 2 | 0,77% | 2 | 0,79% | 2 | 0,78% |
| Bloch & Schneider (1801) | 3 | 0,31% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Cohen et al. (1990) | 3 | 0,31% | 3 | 1,15% | 3 | 1,18% | 3 | 1,17% |
| Cousins et al. (2013) | 3 | 0,31% | 3 | 1,15% | 3 | 1,18% | 3 | 1,17% |
| Cuvier (1829) | 3 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duhamel (1986) | 3 | 0,31% | 3 | 1,15% | 3 | 1,18% | 3 | 1,17% |
| Gill & Townsend (1897) | 3 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goren & Galil (2015) | 3 | 0,31% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Hureau (1966) | 3 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Leach (1818) | 3 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
| Annales de la Société de Sciences naturelles de la Charente-Maritime, 10(2): 225-236.">Quéro et al. (2011) | 3 | 0,31% | 3 | 1,15% | 3 | 1,18% | 3 | 1,17% |
| Balushkin (1996) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barthélémy (1926) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Berrebi et al. (2018) | 2 | 0,21% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Bloch (1795) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonnaterre (1788) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couch (1877) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Denys et al. (2022) | 2 | 0,21% | 2 | 0,77% | 2 | 0,79% | 2 | 0,78% |
| Duhamel (2019) | 2 | 0,21% | 2 | 0,77% | 2 | 0,79% | 2 | 0,78% |
| Garman (1896) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garman (1906) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gilbert (1915) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1883) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1895) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1896) | 2 | 0,21% | 2 | 0,77% | 2 | 0,79% | 2 | 0,78% |
| Günther (1876) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heckel & Kner (1858) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Howell Rivero (1936) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hureau (1966) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iglésias et al. (2020) | 2 | 0,21% | 2 | 0,77% | 2 | 0,79% | 2 | 0,78% |
| Iglesias et al. (2022) | 2 | 0,21% | 2 | 0,77% | 2 | 0,79% | 2 | 0,78% |
| Proceedings of the California Academy of Sciences, 55(10): 190-207.">Iwamoto et al. (2004) | 2 | 0,21% | 2 | 0,77% | 2 | 0,79% | 2 | 0,78% |
| Jordan & Thompson (1914) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1896) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourdan (2020) | 2 | 0,21% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Jung et al. (2024) | 2 | 0,21% | 2 | 0,77% | 2 | 0,79% | 2 | 0,78% |
| Keith et al. (2011) | 2 | 0,21% | 2 | 0,77% | 2 | 0,79% | 2 | 0,78% |
| Lesueur (1821) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe et al. (2007) | 2 | 0,21% | 2 | 0,77% | 2 | 0,79% | 2 | 0,78% |
| Proceedings of the general meetings for scientific business of the Zoological Society of London, 1839: 76-92.">Lowe (1839) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Osório (1909) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pascal et al. (2006) | 2 | 0,21% | 2 | 0,77% | 2 | 0,79% | 2 | 0,78% |
| Poss & Duhamel (1991) | 2 | 0,21% | 2 | 0,77% | 2 | 0,79% | 2 | 0,78% |
| Preynat (2013) | 2 | 0,21% | 2 | 0,77% | 2 | 0,79% | 2 | 0,78% |
| Prirodina (2004) | 2 | 0,21% | 2 | 0,77% | 2 | 0,79% | 2 | 0,78% |
| Reinhardt (1837) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richardson (1844-48) | 2 | 0,21% | 2 | 0,77% | 2 | 0,79% | 2 | 0,78% |
| Richer de Forges et al. (2005) | 2 | 0,21% | 2 | 0,77% | 2 | 0,79% | 2 | 0,78% |
| Risso (1810) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shandikov (2008) | 2 | 0,21% | 2 | 0,77% | 2 | 0,79% | 2 | 0,78% |
| Simian et al. (2022) | 2 | 0,21% | 2 | 0,77% | 2 | 0,79% | 1 | 0,39% |
| Storer (1839) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Straube et al. (2011) | 2 | 0,21% | 2 | 0,77% | 2 | 0,79% | 2 | 0,78% |
| Aboussouan & Rasonarivo (1986) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Anonyme (1996) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2004) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2004) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Audige (1927) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bacchet et al. (2007) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Bennett (1831) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bertin (1928) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 0 | 0% |
| Beslagic et al. (2013) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Bigelow et al. (1953) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch & Schneider (1801) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Bloch (1782-1784) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1784) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1788) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Bonaparte (1837) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cherel et al. (2004) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Collett (1889) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Collett (1904) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Costa (1862) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couteyen (2006) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Cuvier & Valenciennes (1829) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Cuvier & Valenciennes (1846) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1849) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dekay (1842) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dekay (1842) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delrieu-Trottin et al. (2015) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel & Pruvost (2001) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel & Pruvost (2001) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel & Pruvost (2001) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel & Pruvost (2001) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel & Pruvost (2001) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel & Pruvost (2001) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel & Pruvost (2001) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel (1989) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel (1996) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel (1996) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duhamel (1997) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel (1998) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel (1998) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel (1998) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel (1998) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel (1998) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel (1998) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel (1998) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel (1998) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel (1998) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel (1998) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel (1998) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel (1998) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duhamel (1998) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel (2004) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Duhamel (2005) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Faber (1829) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1780) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fleming (1828) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fraser-brunner (1949) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Gargominy et al. (1996) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Garman (1899) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1861) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girard (1855) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girard (1859) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gistel (1848) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1878-1879) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode & Bean (1883) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goode (1881) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1862) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Günther (1864) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1877) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1887) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hector (1875) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hulley (1988) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Hureau & Ozouf-Costaz (1980) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Jordan & Gilbert (1881) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Snyder (1902) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1892) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1894) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keith & Dorson (2003) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Keith & Machino (2003) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Keith et al. (2002) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Keith et al. (2006) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Keith (2002) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Legendre (1942) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesueur (1818) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Letourneur et al. (2004) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Lönnberg (1905) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lorance et al. (2002) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Lowe (1834) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Lowe (1843) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe (1846) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Lütken (1892) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Machino (2003) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Malm (1877) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monod & Dollfus (1932) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Moreau (1881) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nelson-Smith et al. (2014) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Pascal et al. (2003) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Pennant (1787) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pennant (1812) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Perez Canto (1886) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Puissauve, Legros & Poulet (2015) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Rafinesque (1810) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richardson (1843) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richardson (1844) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Rignault & Chevallier (2017) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Roule (1916) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sardou (1980) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Scoresby (1820) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scoresby (1820) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Séret (2014) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shaw (1804) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Spitz et al. (2007) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Storer (1846) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vaillant (1888) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Valenciennes (1836-1844) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Van Guelpen (2016) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Waite (1914) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1934) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1939) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1948) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Williams et al. (2006) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Wood (1848) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yarrell (1839) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zhukov (2020) | 1 | 0,1% | 1 | 0,38% | 1 | 0,39% | 1 | 0,39% |
| Zugmayer (1914) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
